Table 1 |
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Total fatty acid production of synthesized and cloned acyl-ACP TEs |
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|
Kingdom |
Subfamily |
ACC No./Name |
Organism |
Rationale for synthesisa |
Total FAb (nmol/mL) |
|
|
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|
Planta |
A |
AAC49179c, d |
Cuphea palustris |
A (Bimodal specificity for C8 and C10 substrates) [1] |
708 ± 45 |
|
|
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|
AAB71731 |
Ulmus americana |
A (Broad specificity; highest activity on C10 and C16) [13] |
1098 ± 62 |
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|
|
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|
AAG43857 |
Iris germanica |
B |
261 ± 20 |
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|
|
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|
AAG43858 |
Iris germanica |
B |
14.8 ± 4.6 |
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|
|
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|
EER87824 |
Sorghum bicolor |
B (Member of a Subfamily A Poeceae TE cluster) |
126 ± 13 |
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|
|
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|
EER88593 |
Sorghum bicolor |
B (Member of a Subfamily A Poeceae TE cluster) |
90.7 ± 8.0 |
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|
|
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|
CnFatB1 |
Cocos nucifera |
C |
130 ± 12 |
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|
|
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|
CnFatB2 |
Cocos nucifera |
C |
572 ± 32 |
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|
|
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|
CnFatB3 |
Cocos nucifera |
C |
200 ± 11 |
||
|
|
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|
CvFatB1 |
Cuphea viscosissima |
C |
79.2 ± 9.7 |
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|
|
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|
CvFatB2 |
Cuphea viscosissima |
C |
249 ± 9 |
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|
|
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|
CvFatB3 |
Cuphea viscosissima |
C |
18.9 ± 2.1 |
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|
|
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|
AAD42220 |
Elaeis guineensis |
C |
36.7 ± 3.8 |
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|
|
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|
B |
EDQ65090 |
Physcomitrella patens |
B (Member of novel plant subfamily) |
380 ± 29 |
|
|
|
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|
EER96252 |
Sorghum bicolor |
B (Member of novel plant subfamily) |
175 ± 11 |
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|
|
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|
EES11622 |
Sorghum bicolor |
B (Member of novel plant subfamily) |
9.43 ± 2.03 |
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|
|
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|
D |
EEH52851 |
Micromonas pusilla |
B |
16.3 ± 1.6 |
|
|
|
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|
Bacteria |
E |
ACL08376 |
Desulfovibrio vulgaris |
D (Medium-chain linear, branched, and hydroxy fatty acids) [29] |
330 ± 9 |
|
|
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|
F |
CAH09236 |
Bacteroides fragilis |
D (Hydroxy fatty acids) [29] |
215 ± 6 |
|
|
|
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|
ABR43801 |
Parabacteroides distasonis |
D (Branched and branched hydroxy fatty acids) [30] |
70.3 ± 4.4 |
||
|
|
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|
AAO77182e |
Bacteroides thetaiotao- |
D (Anteiso-branched and hydroxy fatty acids) [29] |
60.4 ± 2.9 |
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|
|
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|
micron |
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|
|
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|
G |
ABG82470 |
Clostridium perfringens |
D (Medium-chain fatty acids) [31] |
72.0 ± 9.5 |
|
|
|
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|
H |
EEG55387 |
Clostridium asparagiforme |
B |
25.9 ± 4.2 |
|
|
|
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|
EET61113 |
Bryantella formatexigens |
B |
381 ± 3 |
||
|
|
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|
I |
EDV77528 |
Geobacillus sp. |
D (Iso-branched fatty acids) [32] |
64.9 ± 12.0 |
|
|
|
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|
J |
BAH81730 |
Streptococcus dysgalactiae |
D (Medium-chain and cyclic propane ring fatty acids) [29] |
623 ± 14 |
|
|
|
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|
ABJ63754 |
Lactobacillus brevis |
D (Medium-chain and cyclic propane ring fatty acids) [33] |
710 ± 10 |
||
|
|
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|
CAD63310e |
Lactobacillus plantarum |
436 ± 10 |
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|
|
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|
Non-grouped |
EEI82564 |
Anaerococcus tetradius |
D (Organism produces butyric acid) [35] |
1381 ± 146 |
|
|
|
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|
CAE80300 |
Bdellovibrio bacteriovorus |
D (Straight-chain odd-numbered fatty acids) [29] |
333 ± 18 |
||
|
|
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|
ABN54268 |
Clostridium thermocellum |
D (Branched-chain fatty acids) [29] |
97.7 ± 3.2 |
||
|
|
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|
a A: Functionally characterized TEs; B: TE does not group near characterized TEs and/or no organism lipid profile information is available; C: TEs cloned from organisms known to produce MCFAs; D: Organism's lipid profile used and predominant fatty acid constituents identified in the organism are listed in parentheses. b The data are represented as mean ± standard error (n = 4). c All but the three C. nucifera sequences were codon-optimized for expression in E. coli. d Transit peptides were removed from all plant sequences. e Acyl-ACP TEs with known crystal structures. TEs were expressed in E. coli K27, and free fatty acids (FAs) that accumulated in the medium were analyzed by GC-MS. |
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|
Jing et al. BMC Biochemistry 2011 12:44 doi:10.1186/1471-2091-12-44 |
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